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- source_evidence_literature type ECO_0000212 NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_assertion description "[Recently, another causative gene, CISD2, has been identified in patients with a type of Wolfram syndrome (WS2) resulting in early optic atrophy, diabetes mellitus, deafness, decreased lifespan, but not diabetes insipidus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_assertion evidence source_evidence_literature NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_assertion SIO_000772 22790102 NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_assertion wasDerivedFrom befree-20140225 NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_assertion wasGeneratedBy ECO_0000203 NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP506524.RAP9F9wTzgye998FwyIWCSiB_4Mqf9rhXzvtPY5I_5YT4130_provenance.